4.8 Article

Restoration of vision after transplantation of photoreceptors

期刊

NATURE
卷 485, 期 7396, 页码 99-103

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nature10997

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资金

  1. Medical Research Council UK [G03000341]
  2. Wellcome Trust [082217]
  3. Royal Society [RG080398]
  4. British Retinitis Pigmentosa Society [GR566]
  5. Miller's Trust
  6. Department of Health's National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital
  7. Alcon Research Institute
  8. Great Ormond Street Hospital Children's Charity
  9. US National Institutes of Health [EY06837]
  10. Antonio Champalimaud Vision Award (Portugal)
  11. Research to Prevent Blindness [EY11307, EY016805]
  12. European Research Council
  13. Fight for Sight [1779/80, 1351/52] Funding Source: researchfish
  14. Great Ormond Street Hospital Childrens Charity [V1221, V1257] Funding Source: researchfish
  15. Medical Research Council [G0700438, MR/J004553/1, G0901550, G0800791] Funding Source: researchfish
  16. National Institute for Health Research [NIHR-RP-011-003, NF-SI-0508-10130] Funding Source: researchfish
  17. MRC [G0901550, MR/J004553/1, G0700438, G0800791] Funding Source: UKRI

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Cell transplantation is a potential strategy for treating blindness caused by the loss of photoreceptors. Although transplanted rod-precursor cells are able to migrate into the adult retina and differentiate to acquire the specialized morphological features of mature photoreceptor cells(1), the fundamental question remains whether transplantation of photoreceptor cells can actually improve vision. Here we provide evidence of functional rod-mediated vision after photoreceptor transplantation in adult Gnat1(-/-) mice, which lack rod function and are a model of congenital stationary night blindness(2). We show that transplanted rod precursors form classic triad synaptic connections with second-order bipolar and horizontal cells in the recipient retina. The newly integrated photoreceptor cells are light-responsive with dim-flash kinetics similar to adult wild-type photoreceptors. By using intrinsic imaging under scotopic conditions we demonstrate that visual signals generated by transplanted rods are projected to higher visual areas, including V1. Moreover, these cells are capable of driving optokinetic head tracking and visually guided behaviour in the Gnat1(-/-) mouse under scotopic conditions. Together, these results demonstrate the feasibility of photoreceptor transplantation as a therapeutic strategy for restoring vision after retinal degeneration.

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